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Métodos Terapéuticos y Terapias MTCI
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1.
Parasitol Res ; 117(12): 3979-3991, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30327919

RESUMEN

Nutraceutical plants provide nutrients for the animal as well as secondary compounds that can affect the biology and survival of gastrointestinal nematodes (GIN). Current screening of nutraceutical plants is based on in vitro evidence of anthelmintic (AH) activity against different life stages of GIN, but nutritional information is omitted or scarce. This study proposes an integral in vitro screening protocol to identify the nutraceutical value of the foliage from plant species consumed by small ruminants, using Haemonchus contortus as a biological model. The leaves from Acacia collinsii, A. pennatula, Bunchosia swartziana, Gymnopodium floribundum, Havardia albicans, Leucaena leucocephala, Lysiloma latisiliquum, Mimosa bahamensis, Piscidia piscipula, and Senegalia gaumeri were evaluated for their chemical composition and in vitro digestibility. Acetone:water extracts (70:30) from leaves of each plant were evaluated using the egg hatch assay and larval exsheathment inhibition assay. Respective effective concentrations 50% (EC50) were determined for each assay. The ten plant species showed good nutritional value for ruminants, including crude protein (> 10%), metabolizable energy (> 2.9 MJ/kg DM), and varied CT content (from 1.0 to 37.6%). The best AH activity against H. contortus eggs (EC50 = 401.8 µg/mL) and L3 (EC50 = 83.1 µg/mL) was observed for S. gaumeri extract. Although all the plant species showed in vitro nutraceutical potential, the leaves of S. gaumeri had the best values. The proposed in vitro protocol showed to be useful for the integral assessment of the nutraceutical potential of different plant species as it included the nutritional value and the AH activity against eggs and L3 in the selected plant species.


Asunto(s)
Antihelmínticos/farmacología , Fabaceae/química , Haemonchus/efectos de los fármacos , Larva/efectos de los fármacos , Extractos Vegetales/farmacología , Animales , Suplementos Dietéticos , Enfermedades Gastrointestinales/parasitología , Tracto Gastrointestinal/parasitología , Hojas de la Planta/química , Rumiantes/parasitología , Taninos/análisis
2.
Vet Parasitol ; 228: 121-125, 2016 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-27692312

RESUMEN

Six compounds in a methanolic extract of Petiveria alliacea stem (cis-stilbene; benzyl disulphide; benzyl trisulphide; and methyl esters of hexadecanoic acid, octadecadienoic acid and octadecenoic acid) are known to exercise acaricide activity against cattle tick Rhipicephalus microplus larvae and adults. The synergistic effect of 57 combinations of these six compounds on acaricide activity against R. microplus was evaluated. Larvae immersion tests produced the lethal concentrations needed to kill 50% (LC50) and 99% (LC99) of the population. Adult immersion tests produced rates (%) for mortality, oviposition inhibition and eclosion inhibition. Individually, none of the compounds (1% concentration) exhibited acaricide activity (mortality ≤2.3%). When combined, however, nine mixtures exhibited a synergistic increase in activity, with high mortality rates (≥92%) in larvae. Values for LC50 ranged from 0.07 to 0.51% and those for LC99 from 0.66 to 5.16%. Thirty six compound mixtures had no significant activity (mortality ≤30%) against larvae. Two mixtures exhibited synergism against adults, with high rates (≥92%) of oviposition inhibition. The mixtures based on the benzyl disulphide+benzyl trisulphide pairing produced a synergistic effect against acaricide-resistant R. microplus larva and adults, and are therefore the most promising combination for controlling this ubiquitous ectoparasite.


Asunto(s)
Ácidos Grasos/farmacología , Phytolaccaceae/química , Rhipicephalus/efectos de los fármacos , Estilbenos/farmacología , Sulfuros/farmacología , Acaricidas/farmacología , Animales , Bovinos , Enfermedades de los Bovinos/tratamiento farmacológico , Enfermedades de los Bovinos/parasitología , Resistencia a Medicamentos , Sinergismo Farmacológico , Quimioterapia Combinada , Femenino , Larva/efectos de los fármacos , Oviposición/efectos de los fármacos , Extractos Vegetales/farmacología , Tallos de la Planta/química , Infestaciones por Garrapatas/parasitología , Infestaciones por Garrapatas/prevención & control , Infestaciones por Garrapatas/veterinaria
3.
Nat Prod Res ; 27(17): 1594-7, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23098219

RESUMEN

A phytochemical investigation of the stem bark of Diospyros cuneata (Ebenaceae) together with in vitro cytotoxic evaluation of the pure compounds in four human cancer cell lines KB, Hep-2, HeLa and SiHa led to the isolation of plumbagin, elliptinone, lupeol, atraric acid methyl ester, maritinone, betulin and betulinaldehyde. The structural determination of the compounds was established by nuclear magnetic resonance, electron ionisation mass spectrometric analysis as well as comparison with data from the literature. Plumbagin exhibited a potent cytotoxic activity (CC50 = 3.56 µg mL(-1)) against KB cell lines whereas maritinone displayed cytotoxic activity against Hep-2 (CC50 = 17.30 µg mL(-1)), cervical cancer (CC50 = 21.10 µg mL(-1)) and the KB cell lines (CC50 = 20.30 µg mL(-1)). This is the first report on a phytochemical and biological evaluation of D. cuneata.


Asunto(s)
Diospyros/química , Corteza de la Planta/química , Tallos de la Planta/química , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Humanos , Naftoquinonas/química , Triterpenos Pentacíclicos/química , Extractos Vegetales/química , Extractos Vegetales/farmacología , Triterpenos/química
4.
Vet Parasitol ; 189(2-4): 284-90, 2012 Oct 26.
Artículo en Inglés | MEDLINE | ID: mdl-22579554

RESUMEN

The in vivo anthelmintic (AH) activity of the ethanolic extract from leaves of Phytolacca icosandra was evaluated in goats artificially infected with Haemonchus contortus. Parasite naïve goats were artificially infected with 3000 H. contortus infective larvae per animal. Once the infection was patent (day 28 post-infection) all the animals were sampled to determine the faecal egg counts (FEC) for five consecutive days. Two groups of animals were formed balanced for their FEC and body-weight (BW) (n=6/group): the non-treated control group and the treated group in which goats were individually administered with the ethanolic extract of P. icosandra. The extract was administered orally using gelatin capsules (250 mg/kg BW) which were dosed on two consecutive days using a pill-dispenser. Faecal samples were collected from each animal from the day of dosage (Day 0) on a daily basis to determine the number of eggs per gram of feces (EPG) for 15 days post-treatment (PT). The FEC of the two groups were compared using the repeated measures analyses of variance using the log transformed data Ln (FEC+1). The presence of saponins, coumarins, flavonoids, steroids and terpenoids were detected by standard methodologies in the extract. The P. icosandra ethanolic extract was further analyzed by gas chromatography (GC) coupled to a mass spectrometry (GC-MS). A significant reduction in FEC was observed in the treated group compared to the control from day 7 until day 15 PT (P<0.05). The highest percentage reduction (72%) was found on day 11 PT. No adverse reactions were observed in all treated animals for the entire trial. The GC-MS analysis of the organic extracts revealed the presence of three fatty acids as compounds with highest abundance. The three compounds that were identified by their mass fragmentation patterns were: 2-Pentadecanone, 6, 10, 14-trimethyl (RT 10.3 min), Pentadecanoic acid, 14-methyl-, methyl ester (RT 10.8 min) and Hexadecanoic acid, ethyl ester (RT 11.2 min). It is concluded that the P. icosandra ethanolic extract obtained from leaves showed in vivo anthelmintic activity against H. contortus when administered orally to goats at a dose of 250 mg/kg BW on two consecutive days. The dose used did not cause any negative effects on the health of goats.


Asunto(s)
Antihelmínticos/uso terapéutico , Enfermedades de las Cabras/parasitología , Hemoncosis/tratamiento farmacológico , Haemonchus/efectos de los fármacos , Phytolacca/química , Extractos Vegetales/farmacología , Animales , Heces/parasitología , Enfermedades de las Cabras/tratamiento farmacológico , Cabras , Recuento de Huevos de Parásitos , Extractos Vegetales/química , Hojas de la Planta/química , Factores de Tiempo
5.
Vet Parasitol ; 179(1-3): 100-6, 2011 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-21439732

RESUMEN

The development of anthelmintic resistance has impacted on the success of conventional anthelmintics (AH) for the control of gastrointestinal nematodes in grazing/browsing sheep and goats. Medicinal plants from the traditional herbolary in Mexico may provide new candidates that can be explored as alternative sources of AHs for ruminants. This study evaluated the leaf extracts derived from Phytolacca icosandra against infective L(3) larvae and eggs from Haemonchus contortus collected from sheep. Three extracts of different polarities were obtained from the leaf plants using ethanol, n-hexane and dichloromethane as the solvents. The effectiveness of the in vitro AH activity of the plant extracts was evaluated using larval migration inhibition (LMI) and egg hatch (EHA) assays. For the LMI assays, the ethanolic extract of P. icosandra showed 55.4% inhibition of larval migration at 2mg/mL (p<0.05). The dichloromethane extract of P. icosandra showed 67.1% inhibition of migration at 3mg/mL (p<0.05) and a dose-dependent response with an LD(50) of 0.90 mg/mL. The n-hexane extract failed to show inhibition of larval migration at any concentration explored. In the EHA for the ethanol extract, the lowest concentration tested (0.15 mg/mL) resulted in inhibition of egg hatching greater than 72.6%. Therefore, the LD(50) could not be calculated for this extract. The LD(50) of the dichloromethane extract of P. icosandra was 0. 28 mg/mL. An egg hatch inhibition greater than 90% was observed with both the ethanolic and dichloromethane extracts when using a concentration of 0.90 mg/mL or higher. The n-hexane extract failed to show egg hatch inhibition at any concentration tested. The AH activity reported for P. icosandra could be attributable to the flavonoids, steroids, terpenoids, coumarins and/or saponins that were present in the ethanolic and dichloromethane extracts. A combination of more than one component may also explain the observed AH activity against the H. contortus life stages that were evaluated. In conclusion, the ethanolic and dichloromethane extracts of P. icosandra showed clear in vitro AH activity against the H. contortus eggs and the L(3) larvae. However, the hexanic extract of the plant leaves failed to show any in vitro AH activity.


Asunto(s)
Haemonchus/efectos de los fármacos , Óvulo/efectos de los fármacos , Phytolacca/química , Extractos Vegetales/farmacología , Animales , Larva/efectos de los fármacos , Actividad Motora/efectos de los fármacos , Extractos Vegetales/química
6.
Vet Parasitol ; 168(3-4): 299-303, 2010 Mar 25.
Artículo en Inglés | MEDLINE | ID: mdl-20042296

RESUMEN

The acaricidal activity of crude extracts and fractions from stems and leaves of Petiveria alliacea (Phytolaccaceae) was carried out on larvae and adults of the cattle tick Rhipicephalus (Boophilus) microplus using the larval immersion test (LIT) and adult immersion test (AIT), respectively. Methanolic extracts of stems and leaves of P. alliacea showed 100% mortality on the LIT bioassay. On the other hand, methanolic extracts of leaves and stem on the AIT test showed 26% and 86% of mortality, respectively, egg laying inhibition of 40% and 91%, respectively and hatchability inhibition of 26% and 17%, respectively. Purification of the active stem methanolic extract showed that the activity was present in the n-hexane non-polar fraction. Bioassay-guided purification of the n-hexane fraction produced 10 semi-purified fractions; fraction B had the highest activity against tick larvae (100% mortality). Gas chromatography-mass spectrometry demonstrated that the chemical composition of the active fraction B samples were mainly composed of benzyltrisulfide (BTS) and benzyldisulfide (BDS). These metabolites might be responsible for the acaricidal activity of stem extract of P. alliacea. However, further experiments to evaluate the acaricidal activity of BTS and BDS on larvae and adults of R. (B.) microplus are needed. Our results showed that P. alliacea is a promising biocontrol candidate as acaricide against R. (B.) microplus resistant strains.


Asunto(s)
Acaricidas/farmacología , Phytolaccaceae/química , Extractos Vegetales/farmacología , Rhipicephalus/efectos de los fármacos , Animales , Bovinos , Enfermedades de los Bovinos/parasitología , Femenino , Larva/efectos de los fármacos , Dosificación Letal Mediana , Metanol/química , Oviposición/efectos de los fármacos , Extractos Vegetales/química , Hojas de la Planta/química , Tallos de la Planta/química , Infestaciones por Garrapatas/parasitología , Infestaciones por Garrapatas/veterinaria
7.
Phytomedicine ; 14(7-8): 530-3, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17291734

RESUMEN

A number of flavonoids isolated from Lonchocarpus spp. were evaluated for their antiprotozoal and cytotoxic activity. Flavone 6 and chalcone 7 were found to be the most active against Leishmania parasites and against cell cultures of Leukemia P388DI and adenocarcinoma prostate PC-3.


Asunto(s)
Antineoplásicos Fitogénicos/farmacología , Antiprotozoarios/farmacología , Ciclo Celular/efectos de los fármacos , Derris/química , Flavonas/farmacología , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/toxicidad , Antiprotozoarios/química , Antiprotozoarios/toxicidad , Línea Celular Tumoral , Flavonas/química , Flavonas/toxicidad , Humanos , Leucemia/patología , Masculino , Estructura Molecular , Fitoterapia , Neoplasias de la Próstata/patología
8.
Phytochemistry ; 54(6): 611-4, 2000 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-10963455

RESUMEN

The stem bark of Lonchocarpus xuul (Leguminosae) has yielded four flavonoids which have been identified by spectroscopic methods as the novel 4beta,5-dimethoxy-6",6"-dimethyl-2H-pyrano-(2",3":7,6)-fl avan (xuulanin), 3beta,4beta,5-trimethoxy-6",6"-dimethyl-2H-pyrano-(2",3":7,6 )-flavan (3beta-methoxyxuulanin). 4beta-ethoxy-5-methoxy-6",6"-dimethyl-2H-pyrano-(2",3":7,6)- flavan (4beta-demethylxuulanin-4beta-ethyl ether), and the known 5,7-dihydroxy-6,8-di(3-methylbut-2-enyl)flavanone (spiniflavanone-B). The ethyl derivative is considered likely to be an artefact.


Asunto(s)
Fabaceae/química , Flavonoides/química , Plantas Medicinales , Árboles/química , Flavonoides/aislamiento & purificación , Espectroscopía de Resonancia Magnética
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